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The Relevance Between the microRNA-30e in Plasma and the Prognosis of Schizophrenia Patients

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03007303
Enrollment
30
Registered
2017-01-02
Start date
2016-06-30
Completion date
2020-07-31
Last updated
2020-01-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Micrognathia, Schizophrenia

Brief summary

This study investigates the relationship of circulating microRNA-30e and schizophrenia, and shows the relevance of the aberrant microRNA-30e expression in plasma with the variation disease status.

Detailed description

The plasma samples from 15 individuals with schizophrenia (with a diagnosis of ICD-10) and the equivalent healthy controls will be conducted with the quantification analysis of the microRNA-30e via real-time quantitative polymerase chain reaction(RT-PCR). The 15 patients enrolled should be the first-episode and have not been treated, or were drug free 3 months recently at least. This research measures the expression level of microRNA-30e in schizophrenia respectively before the beginning treatment with atypical psychotics or combined with MECT, after the 4-week treated , the 8-week treated compared with 15 healthy controls.

Interventions

Olanzapine: tablet ,5-20mg, Po q.d. Risperidone: tablet ,1-3 mg, Po q.d. Quetiapine: tablet ,100-400mg, Po b.i.d. ziprasidone : tablet ,40 -80mg, Po b.i.d.

OTHERatypical antipsychotic combined with MECT

The schizophrenia who matches the indications such as severe negativism, refused to eating or stupor may be treated with antipsychotic combined with MECT, the frequency and times of MECT depend on the state of illness

Sponsors

TAKARA BIOTECHNOLOGY(DALIAN)CO.,LTD.
CollaboratorUNKNOWN
Dalian Seventh People's Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
17 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Persons should be diagnosed with schizophrenia according to the International Statistical Classification of Diseases and Related Health Problems 10th Revision (ICD-10) * The first-onset or drug-free in the latest 3 months * Between the ages of 17-40

Exclusion criteria

* Comorbid with other psychosis * Have physical or neurological diseases such as traumatic brain injuries * History of drug-abused or alcoholic * Blood transfusion history in a month * Been treated with Modified Electric Convulsive Therapy(MECT) in late 3 months

Design outcomes

Primary

MeasureTime frameDescription
the Baseline expression profiling of microRNA-30e measured by real-time quantitative poly-chain reaction (QPCR)before the treatmentthe plasma samples will be collected from the patients with schizophrenia and the healthy controls at the beginning recruit for the microRNA-30e detection
the Changed expression level of microRNA-30e measured by real-time quantitative poly-chain reaction (QPCR)Change from Baseline expression level at 4-week treatmentthe plasma samples will be collected from the patients with schizophrenia at the 4-week treatment for the microRNA-30e detection

Secondary

MeasureTime frameDescription
the scores of Positive and Negative Syndrome Scale(PANSS) for the patients with schizophreniabefore, after 4 weeks and 8 weeks treatmentThe PANSS for estimating the severity of positive and negative symptoms in schizophrenia
The degree of Personal and Social Performance scale(PSP) for the patients with schizophreniabefore, after 4 weeks and 8 weeks treatmentThe degree of Personal and Social Performance scale(PSP) used to evaluate the disable levels in Multiple dimensions ,especially in social and self-care performance
The scale of Clinical Global Impression(CGI) in patients with schizophrenia after treatment4 weeks and 8 weeks treatmentMain purpose to provide a global rating of illness severity ,improvement and response to treatment for the patients with schizophrenia

Countries

China

Contacts

Primary ContactGuanghui Fu, postgraduate
fuguanghui1023@126.com86-188 4282 1307
Backup ContactShoufu Xie, postgraduate
doctorxie1023@126.com86-0411 8451 4015

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026